Attention Deficit Hyperactivity Disorder, Bipolar Disorder
Conditions
Keywords
clinical trial, aripiprazole, Bipolar Disorder, Attention-Deficit Hyperactivity Disorder, ADHD
Brief summary
There is a scarcity of clinical trials assessing the effects of medications in children with bipolar disorder. This study aims to assess the efficacy of Aripiprazole (a novel anti-psychotic drug) for the treatment of children and adolescents with bipolar disorder comorbid with ADHD. The study design is a 8-week randomized, double blind, parallel group trial. Patients were randomized to either aripiprazole or placebo. The main hypotheses are: 1. Aripiprazole will significantly reduce maniac scores compared to placebo 2. Aripiprazole will significantly reduce ADHD scores compared to placebo
Detailed description
Bipolar disorder (BD) is a chronic disorder that severely affects the normal development of children and adolescents. The disorder is associated with high rates of suicide tentative and high-risk behaviors like sexual promiscuity and drug abuse. Bipolar disorder in children is also associated with high rates of comorbidity, especially with Attention-Deficit Hyperactivity Disorder (ADHD). There is a scarcity of clinical trials assessing the effects of medications in children with BD. Moreover, the frequent presence of comorbid ADHD might determine lower response to treatment. Aripiprazole is a novel anti-psychotic drug. Its mechanism of action seems to be related to a stabilization of dopaminergic transmission, acting as a partial agonist especially in dopaminergic D2 receptors. It also has effects in 5-HT1a serotonergic receptors. Thus, it might have a promising effect in children and adolescents with comorbid BD and ADHD. A retrospective chart review, recently published, suggests the efficacy of this drug in children with BD. This study aims to assess the efficacy of Aripiprazole (a novel anti-psychotic drug) for the treatment of 50 children and adolescents (age range: 08 to 17 years-old) with Bipolar Disorder comorbid with ADHD. The study design is an 6-week randomized, double blind, parallel group trial. Patients were randomized to either aripiprazole or placebo. The hypotheses are: 1) Aripiprazole will significantly reduce maniac scores compared to placebo; 2)Aripiprazole will significantly reduce ADHD scores compared to placebo; 3) Aripiprazole will not be significantly associated to weight gain compared to placebo.
Interventions
Sponsors
Study design
Eligibility
Inclusion criteria
* Age: 8-17 * BD type I or II comorbid with ADHD * Baseline score in the YMRS \> or = 20
Exclusion criteria
* IQ \< 70 * Pharmacologic treatment in the last month * Pregnancy or absence of a contraceptive method in fertile girls * Diagnoses: pervasive development disorder, schizophrenia, drug abuse or dependency * Risk of suicide or homicide * Clinical condition that might interfere in the study * Known sensibility to aripiprazole
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Scores in the Young Mania Rating Scale (BD) | — |
| Scores in the SNAP-IV (ADHD) | — |
| Weight | — |
Secondary
| Measure | Time frame |
|---|---|
| Scores in the Kutcher Adolescent Depression Scale | — |
| Scores in the CMRS-P | — |
| Report of side events | — |
| Scores of quality of life (YQOL-R) | — |
| Scores in CGI | — |
| Scores in the CDRS | — |
Countries
Brazil